Canonical Allele Identifier: CA519278154

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153648600A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420261A>T , CM000685.2:g.154420261A>T	GRCh38
NC_000023.10:g.153648600A>T , CM000685.1:g.153648600A>T	GRCh37
NC_000023.9:g.153301794A>T	NCBI36
NG_009634.1:g.13724A>T
NG_009634.2:g.13727A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1506A>T
ENST00000698317.1:n.2122A>T
ENST00000698318.1:n.1905A>T
ENST00000698319.1:n.1268A>T
ENST00000698320.1:n.1156A>T
ENST00000470127.2:n.1169A>T
ENST00000475699.6:c.660A>T	ENSP00000419854.3:p.Gly220=
ENST00000483674.3:n.578A>T
ENST00000601016.6:c.696A>T MANE Select	ENSP00000469981.1:p.Gly232=
ENST00000612012.5:c.654A>T	ENSP00000482070.2:p.Gly218=
ENST00000612460.5:c.606A>T	ENSP00000481037.1:p.Gly202=
ENST00000614595.2:n.2043A>T
ENST00000615658.5:n.1285A>T
ENST00000616020.5:c.708A>T	ENSP00000483636.2:p.Gly236=
ENST00000617701.5:c.*709A>T	ENSP00000481645.1:n.*709A>T
ENST00000652354.1:c.378A>T	ENSP00000498734.1:p.Gly126=
ENST00000652358.1:c.489A>T	ENSP00000498464.1:p.Gly163=
ENST00000652390.1:c.615A>T	ENSP00000498858.1:p.Gly205=
ENST00000652476.1:n.1362A>T
ENST00000652644.1:c.309A>T	ENSP00000498496.1:p.Gly103=
ENST00000652682.1:c.753A>T	ENSP00000498288.1:p.Gly251=
ENST00000652685.1:n.1049A>T
ENST00000369776.8:c.606A>T	ENSP00000358791.4:p.Gly202=
ENST00000426231.5:c.693A>T
ENST00000475699.5:c.654A>T	ENSP00000419854.2:p.Gly218=
ENST00000494912.5:n.1385A>T
ENST00000498029.1:n.154A>T
ENST00000601016.5:c.696A>T	ENSP00000469981.1:p.Gly232=
ENST00000612460.4:c.606A>T	ENSP00000481037.1:p.Gly202=
ENST00000613002.4:c.564A>T	ENSP00000478154.1:p.Gly188=
ENST00000615986.4:c.*424A>T	ENSP00000480133.1:n.*424A>T
NM_000116.4:c.696A>T	NP_000107.1:p.Gly232=
NM_001303465.1:c.708A>T	NP_001290394.1:p.Gly236=
NM_181311.3:c.606A>T	NP_851828.1:p.Gly202=
NM_181312.3:c.654A>T	NP_851829.1:p.Gly218=
NM_181313.3:c.564A>T	NP_851830.1:p.Gly188=
NR_024048.2:n.1038A>T
XM_006724836.1:c.750A>T	XP_006724899.1:p.Gly250=
XM_006724837.1:c.735A>T	XP_006724900.1:p.Gly245=
XM_006724839.1:c.618A>T	XP_006724902.1:p.Gly206=
XM_006724841.2:c.489A>T	XP_006724904.1:p.Gly163=
XM_006724842.2:c.399A>T	XP_006724905.1:p.Gly133=
XM_011531189.1:c.537A>T	XP_011529491.1:p.Gly179=
XM_011531190.1:c.489A>T	XP_011529492.1:p.Gly163=
XM_011531191.1:c.420A>T	XP_011529493.1:p.Gly140=
XM_011531192.1:c.417A>T	XP_011529494.1:p.Gly139=
XR_938511.1:n.1044A>T
XM_006724841.4:c.489A>T	XP_006724904.1:p.Gly163=
XM_006724842.4:c.399A>T	XP_006724905.1:p.Gly133=
XM_011531191.2:c.420A>T	XP_011529493.1:p.Gly140=
XM_017029761.1:c.681A>T	XP_016885250.1:p.Gly227=
XM_017029762.1:c.660A>T	XP_016885251.1:p.Gly220=
XM_017029763.1:c.483A>T	XP_016885252.1:p.Gly161=
XM_017029764.1:c.417A>T	XP_016885253.1:p.Gly139=
XM_017029765.2:c.357A>T	XP_016885254.1:p.Gly119=
XM_024452431.1:c.654A>T	XP_024308199.1:p.Gly218=
NM_000116.5:c.696A>T MANE Select	NP_000107.1:p.Gly232=
NM_001303465.2:c.708A>T	NP_001290394.1:p.Gly236=
NM_181311.4:c.606A>T	NP_851828.1:p.Gly202=
NM_181312.4:c.654A>T	NP_851829.1:p.Gly218=
NM_181313.4:c.564A>T	NP_851830.1:p.Gly188=
NR_024048.3:n.1017A>T